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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Page: 1 2 3 4 5 6 7 8 Hits 41 – 60 of 143 41 Multi-parameter machine learning approach to the neuroanatomical basis of developmental dyslexia Płoński, Piotr; Gradkowski, Wojciech; Altarelli, Irene... In: ISSN: 1065-9471 ; EISSN: 1097-0193 ; Human Brain Mapping ; https://hal.archives-ouvertes.fr/hal-01400559 ; Human Brain Mapping, Wiley, 2016 (2016) BASE Show details 42 The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition Hippolyte, Loyse; Maillard, Anne M.; Rodriguez-Herreros, Borja; Pain, Aurelie; Martin-Brevet, Sandra; Ferrari, Carina; Conus, Philippe; Mace, Aurelien; Hadjikhani, Nouchine; Metspalu, Andres; Reigo, Anu; Kolk, Anneli; Maennik, Katrin; Barker, Mandy; Isidor, Bertrand; Le Caignec, Cedric; Mignot, Cyril; Schneider, Laurence; Mottron, Laurent; Keren, Boris; David, Albert; Doco-Fenzy, Martine; Gerard, Marion; Bernier, Raphael; Goin-Kochel, Robin P.; Hanson, Ellen; Snyder, Leeanne Green; Ramus, Franck; Beckmann, Jacques S.; Draganski, Bogdan; Reymond, Alexandre; Jacquemont, Sebastien In: http://infoscience.epfl.ch/record/222363 (2016) Abstract: BACKGROUND: Deletions and duplications of the 16p11.2 BP4-BP5 locus are prevalent copy number variations (CNVs), highly associated with autism spectrum disorder and schizophrenia. Beyond language and global cognition, neuropsychological assessments of these two CNVs have not yet been reported. METHODS: This study investigates the relationship between the number of genomic copies at the 16p11.2 locus and cognitive domains assessed in 62 deletion carriers, 44 duplication carriers, and 71 intrafamilial control subjects. RESULTS: IQ is decreased in deletion and duplication carriers, but we demonstrate contrasting cognitive profiles in these reciprocal CNVs. Deletion carriers present with severe impairments of phonology and of inhibition skills beyond what is expected for their IQ level. In contrast, for verbal memory and phonology, the data may suggest that duplication carriers outperform intrafamilial control subjects with the same IQ level. This finding is reminiscent of special isolated skills as well as contrasting language performance observed in autism spectrum disorder. Some domains, such as visuospatial and working memory, are unaffected by the 16p11.2 locus beyond the effect of decreased IQ. Neuroimaging analyses reveal that measures of inhibition covary with neuroanatomic structures previously identified as sensitive to 16p11.2 CNVs. CONCLUSIONS: The simultaneous study of reciprocal CNVs suggests that the 16p11.2 genomic locus modulates specific cognitive skills according to the number of genomic copies. Further research is warranted to replicate these findings and elucidate the molecular mechanisms modulating these cognitive performances. URL: http://infoscience.epfl.ch/record/222363 https://doi.org/10.1016/j.biopsych.2015.10.021 BASE Hide details 43 Relationship between early language skills and the development of inattention/hyperactivity symptoms during the preschool period: Results of the EDEN mother-child cohort Peyre, Hugo; Galera, Cedric; Van Der Waerden, Judith... In: ISSN: 1471-244X ; BMC Psychiatry ; https://www.hal.inserm.fr/inserm-01393701 ; BMC Psychiatry, BioMed Central, 2015, 16 (1), pp.380. ⟨10.1186/s12888-016-1091-3⟩ (2015) BASE Show details 44 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort Becker, Jessica; Czamara, Darina; Scerri, Tom S. - 2015 BASE Show details 45 Predicting changes in language skills between 2 and 3 years in the EDEN mother–child cohort Peyre, Hugo; Bernard, Jonathan,; Forhan, Anne... In: ISSN: 2167-8359 ; PeerJ ; https://hal.archives-ouvertes.fr/hal-01071489 ; PeerJ, PeerJ, 2014, pp.335. ⟨10.7717/peerj.335⟩ (2014) BASE Show details 46 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort Becker, Jessica; Czamara, Darina; Scerri, Tom S.. - 2014 BASE Show details 47 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort Becker, Jessica; Czamara, Darina; Scerri, Tom S. - : Nature Publishing Group, 2014 BASE Show details 48 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort Becker, Jessica; Czamara, Darina; Scerri, Tom S. - 2014 BASE Show details 49 Genetic basis of language : insights from developmental dyslexia Ramus, Franck In: Birdsong, speech and language (Cambridge, 2013), p. 471-486 MPI für Psycholinguistik Show details 50 Genetic basis of language : insights from developmental dyslexia Ramus, Franck In: Birdsong, speech and language (Cambridge, 2013), p. 471-486 MPI für Psycholinguistik Show details 51 Impaired auditory sampling in dyslexia: further evidence from combined fMRI and EEG Lehongre, Katia; Morillon, Benjamin; Giraud, Anne-Lise... In: ISSN: 1662-5161 ; Frontiers in Human Neuroscience ; https://hal.sorbonne-universite.fr/hal-01557287 ; Frontiers in Human Neuroscience, Frontiers, 2013, 7, pp.454. ⟨10.3389/fnhum.2013.00454⟩ (2013) BASE Show details 52 Predictors of developmental dyslexia in European orthographies with varying complexity. Landerl, Karin; Ramus, Franck; Moll, Kristina... In: ISSN: 0021-9630 ; EISSN: 1469-7610 ; Journal of Child Psychology and Psychiatry ; https://hal.archives-ouvertes.fr/hal-00965034 ; Journal of Child Psychology and Psychiatry, Wiley, 2013, 54 (6), pp.686-94. ⟨10.1111/jcpp.12029⟩ (2013) BASE Show details 53 Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. Becker, Jessica; Czamara, Darina; Scerri, Tom S... In: ISSN: 1018-4813 ; EISSN: 1476-5438 ; European Journal of Human Genetics ; https://hal.archives-ouvertes.fr/hal-00964958 ; European Journal of Human Genetics, Nature Publishing Group, 2013, epub ahead of print. ⟨10.1038/ejhg.2013.199⟩ (2013) BASE Show details 54 Cognitive mechanisms underlying reading and spelling development in five European orthographies Moll, L.; Ramus, Franck; Bartling, J.... In: ISSN: 0959-4752 ; Learning and Instruction ; https://hal.archives-ouvertes.fr/hal-00965264 ; Learning and Instruction, Elsevier, 2013, 29, pp.65-77. ⟨10.1016/j.learninstruc.2013.09.003⟩ (2013) BASE Show details 55 Neurogenetics and auditory processing in developmental dyslexia Giraud, Anne-Lise; Ramus, Franck In: ISSN: 0959-4388 ; Current Opinion in Neurobiology ; https://hal.archives-ouvertes.fr/hal-01074961 ; Current Opinion in Neurobiology, Elsevier, 2013, 23, pp.37 - 42. ⟨10.1016/j.conb.2012.09.003⟩ (2013) BASE Show details 56 Phonological deficits in specific language impairment and developmental dyslexia: towards a multidimensional model Ramus, Franck; Marshall, Chloe R.; Rosen, Stuart. - : Oxford University Press, 2013 BASE Show details 57 Phonological deficits in specific language impairment and developmental dyslexia: towards a multidimensional model Ramus, Franck; Marshall, Chloe R.; Rosen, Stuart. - : Oxford University Press, 2013 BASE Show details 58 Developmental dyslexia: the difficulties of interpreting poor performance, and the importance of normal performance Ramus, Franck; Ahissar, Merav In: Cognitive neuropsychology. - Abingdon : Routledge, Taylor & Francis Group 29 (2012) 1-2, 104-122 BLLDB OLC Linguistik Show details 59 Processing of vocalizations in humans and monkeys: A comparative fMRI study Joly, Olivier; Pallier, Christophe,; Ramus, Franck... In: ISSN: 1053-8119 ; EISSN: 1095-9572 ; NeuroImage ; https://hal.archives-ouvertes.fr/hal-02327524 ; NeuroImage, Elsevier, 2012, 62 (3), pp.1376-1389. ⟨10.1016/j.neuroimage.2012.05.070⟩ (2012) BASE Show details 60 Altered low-γ sampling in auditory cortex accounts for the three main facets of dyslexia. Lehongre, Katia; Ramus, Franck; Villiermet, Nadège... In: ISSN: 0896-6273 ; Neuron ; https://hal.inria.fr/hal-00795726 ; Neuron, Elsevier, 2011, 72 (6), pp.1080-1090. ⟨10.1016/j.neuron.2011.11.002⟩ (2011) BASE Show details Page: 1 2 3 4 5 6 7 8

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